ClearanceBrief
510(k) K921308 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

HG MULTILOCK HIP PROSTHESIS W/ TI-NIDIUM

ApplicantZimmer, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Feb 22, 1994
ReceivedMar 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K921308

DateFirm and productCodeLinked 510(k)
Feb 20, 2014Zimmer, Inc.
HGP II ACETABULAR CUP MOD
Terminated
LPHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.